Canonical Allele Identifier: PA1139744312
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 954171
ClinVar RCV Id: RCV001226581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Gln661Leu
CA399978449
NM_001377265.1:c.1982A>T